HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233587_55233588delinsAC , CM000667.2:g.55233587_55233588delinsAC | GRCh38 |
NC_000005.9:g.54529415_54529416delinsAC , CM000667.1:g.54529415_54529416delinsAC | GRCh37 |
NC_000005.8:g.54565172_54565173delinsAC | NCBI36 |
NG_034201.1:g.5130_5131delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.-65_-64delinsGT MANE Select | ENSP00000282572.4:n.-65_-64delinsGT | |
ENST00000282572.4:c.-65_-64delinsGT | ENSP00000282572.4:n.-65_-64delinsGT | |
ENST00000501463.2:c.-65_-64delinsGT | ENSP00000422485.1:n.-65_-64delinsGT | |
NM_021147.4:c.-65_-64delinsGT | NP_066970.3:n.-65_-64delinsGT | |
NR_125346.1:n.130_131delinsGT | ||
NR_125347.1:n.130_131delinsGT | ||
NM_021147.5:c.-65_-64delinsGT MANE Select | NP_066970.3:n.-65_-64delinsGT | |
NR_125346.2:n.21_22delinsGT | ||
NR_125347.2:n.21_22delinsGT |